| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:79991196-79991347 | Rare:49 | ||||
| chr5:80255910-80256277 | Common:4; Rare:146 | ||||
| chr5:80407872-80408121 | Common:1; Rare:87 | ||||
| chr5:80487896-80488118 | Common:1; Rare:72 | ||||
| chr5:80654112-80654214 | Rare:25 | ||||
| chr5:80654562-80654751 | Common:5; Rare:118 | ||||
| chr5:81233009-81233339 | Common:1; Rare:68 | ||||
| chr5:81301462-81301677 | Common:5; Rare:74 | ||||
| chr5:81751028-81751451 | Common:1; Rare:121 | ||||
| chr5:82278319-82278692 | Common:4; Rare:121 | ||||
| chr5:83077331-83077615 | Common:1; Rare:84 | ||||
| chr5:84384216-84384283 | Rare:23 | ||||
| chr5:84384361-84384737 | Rare:143 | ||||
| chr5:86618326-86618401 | Rare:16 | ||||
| chr5:87267722-87268515 | Common:6; Rare:236; Clinvar:2; Clinvar (benign):2 |